Canonical Allele Identifier: CA2000617619

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228604A= , CM000673.2:g.112228604A=	GRCh38
NC_000011.9:g.112099327A= , CM000673.1:g.112099327A=	GRCh37
NC_000011.8:g.111604537A=	NCBI36
NG_008743.1:g.7240A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.94A= MANE Select	ENSP00000280362.3:p.Ser32=
ENST00000280362.7:c.94A=	ENSP00000280362.3:p.Ser32=
ENST00000524931.1:c.-111A=	ENSP00000434688.1:n.-111A=
ENST00000525645.1:n.169A=
ENST00000525803.1:c.94A=	ENSP00000431750.1:p.Ser32=
ENST00000528679.5:c.94A=	ENSP00000435895.1:p.Ser32=
ENST00000531673.5:c.94A=	ENSP00000433469.1:p.Ser32=
NM_000317.2:c.94A=	NP_000308.1:p.Ser32=
NM_000317.3:c.94A= MANE Select	NP_000308.1:p.Ser32=